1] Center for Brain Immunology and Glia (BIG), Department of Neuroscience, University of Virginia, Charlottesville, VA, USA [2] Microbiology Infectious Disease and Immunology Graduate Program, University of Virginia, Charlottesville, VA, USA.
Center for Brain Immunology and Glia (BIG), Department of Neuroscience, University of Virginia, Charlottesville, VA, USA.
Mol Psychiatry. 2014 May;19(5):531-3. doi: 10.1038/mp.2013.79. Epub 2013 Jun 11.
The traditional view of the central nervous system (CNS) as an immune-privileged organ yielded a longstanding perception of such interactions—as seen for example in multiple sclerosis (MS) —as intrinsically destructive. This notion is changing with the identification of several homeostatic functions attributable to beneficial T-cell/CNS interaction , for example in hippocampal-dependent learning and stress response paradigms , and in models of neurodegeneration and CNS injury . Here we provide insights into the maintenance, and dynamics of the meningeal T-cell repertoire. We show that meningeal T-cell composition is coupled to the CNS-draining deep cervical lymph nodes (dCLNs), whose surgical removal interrupted the normal flow of meningeal T-cells and resulted in cognitive impairment.
传统观点认为中枢神经系统(CNS)是一个免疫特惠器官,因此长期以来人们一直认为这种相互作用——如多发性硬化症(MS)中所见——本质上是具有破坏性的。随着对有益的 T 细胞/中枢神经系统相互作用归因于几种稳态功能的认识的改变,这种观念正在发生变化,例如在海马依赖学习和应激反应范式中,以及在神经退行性变和中枢神经系统损伤模型中。在这里,我们深入了解脑膜 T 细胞库的维持和动态。我们表明,脑膜 T 细胞的组成与中枢神经系统引流的深部颈淋巴结(dCLN)相关,其手术切除中断了脑膜 T 细胞的正常流动,并导致认知障碍。